Safety and Effectiveness of CNDO 201Trichuris Suis Ova (TSO) for the Treatment of Moderate to Severe Plaque Psoriasis

Mark Lebwohl

Status and phase

Completed

Phase 1

Conditions

Psoriasis

Treatments

Drug: TSO 7500

Drug: TSO 2500

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT01836939

GCO 12-1881

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and effectiveness of CNDO 201Trichuris suis ova (TSO) for the treatment of moderate to severe plaque psoriasis.

Full description

The purpose of this study is to evaluate the safety and effectiveness of CNDO 201Trichuris suis ova (TSO) for the treatment of moderate to severe plaque psoriasis.

Psoriasis is driven by T-cell infiltration in the epidermis. The T-cells involved in psoriasis exhibit a Th17-like and a Th1-like cytokine secretion profile. This excess Th17/Th1 response is thought to play a critical role in the development of psoriasis, and reducing Th17/Th1 activity would be a potential way of halting the inflammatory process leading to psoriasis.

Enrollment

8 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Males or females, 18 to 75 years old.
Diagnosis of stable plaque type psoriasis for at least 6 months prior to baseline
Baseline moderate to severe psoriasis, defined as both of the following:
1. Psoriasis covering a body surface area (BSA) ≥ 10%, and;
2. PGA ≥ 3, and;
3. PASI ≥ 12
Must be in good health (except for psoriasis and psoriatic arthritis) as judged by the Investigator, based on medical history, physical examination, and clinical laboratories
In the opinion of the investigator, must be a candidate for systemic therapy or phototherapy of psoriasis
If a woman, before entry she must be:
1. Postmenopausal, defined as 45 years of age with amenorrhea for at least 18 months, or > 45 years of age with amenorrhea for at least 6 months and a serum follicle stimulating hormone (FSH) level > 40 IU/mL, or Surgically postmenopausal (bilateral oophorectomy), or
2. Surgically sterile (have had a hysterectomy or tubal ligation or otherwise be incapable of pregnancy), or
3. If heterosexually active, practicing a highly effective method of birth control, including hormonal prescription oral contraceptives, contraceptive injections, contraceptive patch, intrauterine device, double-barrier method (eg, condoms, diaphragm, or cervical cap, with spermicidal foam, cream, or gel), or male partner sterilization, consistent with local regulations regarding the use of birth control methods for subjects participating in clinical trials, for the duration of their participation in the study and for 2 months after receiving the last administration of any study agent, or
4. Not heterosexually active
Women of childbearing potential must have a negative pregnancy test (urine and serum) prior to randomization
Agree to avoid prolonged exposure to natural sunlight or tanning beds or phototherapy devices for the duration of the study
Agree to avoid any prohibited concomitant medications as detailed below for the duration of the study and for 4 weeks prior to baseline unless indication otherwise
Negative stool culture.
Patient has the ability to provide informed consent.

Exclusion criteria

Patients with known history of intestinal parasitic infection, even if adequately treated, in the past 5 years.
Patient received antibiotic, antifungal or antiparasitic medication in the last 2 weeks prior to Screening and/or would potentially require this during the study treatment period.
Patient with history of drug or alcohol abuse within 6 months prior to Screening.
Patient with evidence of poor compliance with medical advice and instruction including diet or medication.
Patient is unable or unwilling to swallow study medication suspension.
Patient with a significant medical condition which puts the patient at risk for study participation and/or for any reason is considered by the Investigator to be an unsuitable candidate to receive TSO or is potentially put at risk by study procedures.
Patients who has participated in another clinical trial within 30 days of Screening for this trial and/or any experimental treatment for this population.
White blood cell count ≤ 3,000/mm3 (≤ 3.0 x 109/L) or ≥ 14,000/mm3 (≥14 x 109/L)
Platelet count ≤ 100,000/μL (≤100 x 109/L)
Serum creatinine >2 x upper limit of normal (ULN)
AST (SGOT) or ALT (SGPT) > 2 x ULN
Total bilirubin >2 mg/dL (34 μmol/L)
Hemoglobin < 9 g/dL
Patients who are currently taking or have taken in the past 30 days, for any reason, any medication that, in the opinion of the investigator, suppressed the immune response. This may include but is not limited to systemic steroids, azathioprine, cyclosporine, FK506, mycophenolate mofetil, mycophenolic acid, etanercept, adalimumab, infliximab, ustekinumab, cimzia, or any other biologic agent targeted to any cell or cytokine in the immune system.
Patients who are refractory to 2 or more biological agent plaque psoriasis therapies due to lack of efficacy.
Patients currently taking or who have taken in the past 2 weeks, topical steroids.
Patients on a non-stable dose of vitamin D analog in the past 30 days.
Patients currently taking or who have taken in the past 30 days any medications likely to improve psoriasis and thus interfere with evaluation. This may include, in addition to the medications listed above, phototherapy, methotrexate, hydroxyurea, or acitretin.
Patients with a diagnosis of inflammatory bowel disease (ulcerative colitis or Crohn's disease) or of irritable bowel syndrome
Patients with HIV-1/HIV-2 antibody, hepatitis B surface antigen, hepatitis C antibody.
Patient received non-steroidal anti-inflammatory drugs (NSAIDS) within 2 weeks before Baseline visit for more than 3 consecutive days, except acetylsalicylic acid ≤ 350 mg/d which is allowed.
Women who are pregnant, intending to become pregnant, breastfeeding or planning to breastfeed during the study.